Diethylamine → HCID 9951702, compound
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:19]=[C:18]([CH2:20][CH2:21][C:22]([OH:24])=O)[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[N:11]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].C(N1C=CN=C1)(N1C=CN=C1)=O.[CH2:37]([NH:39][CH2:40][CH3:41])[CH3:38]>O1CCCC1>[CH2:37]([N:39]([CH2:40][CH3:41])[C:22](=[O:24])[CH2:21][CH2:20][C:18]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[N:11]=[C:10]([C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)[N:19]=1)[CH3:38]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The procedure is as in Example 7, starting with 2-(4-nitrophenyl)-4-quinazolinepropanoic acid (1.35 g), carbonyldiimidazole (0.82 g) and diethylamine (0.9 cc) in anhydrous tetrahydrofuran (20 cc). After chromatography on silica gel with ethyl acetate as eluant, and recrystallization in ethyl acetate, N,N-diethyl-2-(4-nitrophenyl)-4-quinazolinepropanamide (0.35 g), m.p. 168° C., is obtained.
Workup
- customAfter chromatography on silica gel with ethyl acetate as eluant, and recrystallization in ethyl acetate
Sources & evidence
- ORD record
- ord-16d36a9dc1fc404a881be9cdecbfc105
- Source dataset
- uspto-grants-1988_11
- Patent number
- US04788199
Reaction notes
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